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Investigator Support Assistant

Labcorp
Labcorp
1-3 years
Not Disclosed
Bangalore, India
10 Feb. 13, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Investigator Support Assistant

Job ID: 261919

Location: Bangalore, Karnataka, India

Employment Type: Full-Time | On-Site

Department: Lab Operations

Job Category: Clinical Trial Support | Investigator Services | Lab Operations

Experience Required: 1–3 years in clinical trial support, investigator coordination, or lab operations


About the Company

Labcorp is a leading global life sciences company specializing in clinical trials, diagnostics, and laboratory services. With a commitment to advancing health and improving lives, Labcorp provides innovative solutions to support clinical research, laboratory testing, and patient safety worldwide.


Role Overview

The Investigator Support Assistant will provide critical operational support to the Global Investigator Support (GIS) team by managing workflow, maintaining documentation, and ensuring seamless communication with investigator sites. The role requires attention to detail, strong organizational skills, and a focus on patient safety.

This position is key in supporting clinical trial operations by facilitating sample logistics, resolving site queries, and maintaining compliance with departmental and company standards.


Key Responsibilities

  • Ensure patient safety is prioritized in all day-to-day operations and escalate safety issues promptly

  • Manage timely communication with investigator sites and representatives via email or other assigned workflows

  • Support GIS coordinators with administrative responsibilities, including sample shipment documentation and airway bill preparation

  • Follow up on misdelivered samples and coordinate with relevant departments for resolution

  • Assist investigator sites with portal login issues, access questions, and procedural clarifications

  • Compile and communicate updates to investigator sites regarding new policies or procedures

  • Search, update, and maintain investigator site database records for follow-ups and escalations

  • Resolve simple to moderate system hold issues and answer project-related queries from sites

  • Document service failures and escalate unresolved issues to management

  • Maintain and update training folders, SOPs, and departmental documentation

  • Track and report workflow data according to management requirements

  • Complete onboarding, mandatory corporate, and departmental trainings

  • Participate in ongoing training initiatives regarding process and system updates

  • Perform any additional duties assigned by supervisors to support GIS and lab operations


Required Experience

  • 1–3 years of experience in clinical trial support, investigator services, or lab operations

  • Familiarity with clinical trial workflows, sample logistics, and site coordination

  • Knowledge of SOPs, regulatory compliance, and quality documentation

  • Strong communication, organizational, and problem-solving skills


Educational Qualifications

  • Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related field preferred